CDG ? Consulting, contracting, and training for medical devices.

Gantt chart for a typical clinical research trial; tasks are plotted against time. Click on a task to see how CDG can help you.   
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Biological Safety Biologycal Safety
Market Assessment Market Assessment
Regulatory strategy Regulatory Strategy
Protocol Protocol
Sample size Sample Size
Case report form design Case Report Form Design
Investigator Agreement INvestigators Agreement    
Budget & payment terms Budget and payment terms
Clinical Trials Agreement Clinical Trials Agreement
IRB Review & approval IRB Review and approvalmilestone1  
Initiation, first subject in milestone2
Monitoring close-out las subject out  
Close-out, last subject out milestone3
Database Design Database Design
Data entry, queries Statistical analysismilestone4  
Statistical analysis Regulatory submission, approval  
Regulatory Submission, approval Medical device to market  
TO MARKET

milestone5
Project Management
Training

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773-489-5706

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cdginc@clinicaldevice.com
CDG: consulting, CRO contracting, and training for medical devices and in vitro diagnostics. We do clinical research, contract research, biological safety, biocompatibility, and regulatory consulting. We offer professional development, clinical trial workshops, and e conferences with guest expert speakers, both public and on-site.